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Filtered Search Results
Medchemexpress LLC Carbonic Anhydrase 2 10ug
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Carbonic Anhydrase 2 Protein is a member of the carbonic anhydrase isozyme family responsible for catalyzing the reversible hydration of carbon dioxide Mutations in CA2 are linked to osteopetrosis and renal tubular acidosis The gene exhibits biased expression in various tissues notably in the stomach and colon CA2 plays vital role in the regulation of ion transport and pH balance and is involved in many biological processes Carbonic Anhydrase 2 Protein Mouse (HEK293 His) is the recombinant mouse-derived Carbonic Anhydrase 2 protein expressed by HEK293 with C-His labeled tag
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Medchemexpress LLC Azido-PEG10-Boc | 2490419-48-0 | >98% | C27H53N3O12 | 50 MG
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Azido-PEG10-Boc | 2490419-48-0 | >98% | C27H53N3O12 | 50 MG
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Medchemexpress LLC Boc-NH-PEG12-CH2CH2COOH | 1415981-79-1 | 98.0% | C32H63NO16 | 50 MG
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Boc-NH-PEG12-CH2CH2COOH is a PEG-based PROTAC linker primarily utilized in the synthesis of PROTACs. These innovative molecules leverage the intracellular ubiquitin-proteasome system to selectively degrade target proteins by employing two different ligands connected by a linker: one binds to an E3 ubiquitin ligase, and the other targets the protein intended for degradation.
- Utilized in the synthesis of PROTACs
- Leverages the intracellular ubiquitin-proteasome system to selectively degrade target proteins
- Supplied as a colorless to light yellow liquid
- Density of 1.121 g/cm³
- Recommended storage at -20°C, protected from light
- For longer periods in solvent, store at -80°C
- Exhibits good solubility in DMSO (100 mg/mL)
- Intended for research use only
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![Medchemexpress LLC D-alanine, 3-amino-N-[(1,1-dimethylethoxy)carbonyl] | 76387-70-7 | MFCD01632072 | >97.0% | 204.22 | C8H16N2O4 | 10 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000302632.png-250.jpg)
Medchemexpress LLC D-alanine, 3-amino-N-[(1,1-dimethylethoxy)carbonyl] | 76387-70-7 | MFCD01632072 | >97.0% | 204.22 | C8H16N2O4 | 10 G
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Boc-D-2,3-diaminopropionic acid is a Boc-protected amino acid derivative used in peptide synthesis and small-molecule research; it is supplied as a high-purity solid suitable for laboratory applications.
- Boc-protected amino acid for peptide and small-molecule synthesis.
- Molecular formula C8H16N2O4, molecular weight 204.22.
- Purity ≥97.0% for research use.
- White to off-white solid appearance.
- Available in multiple laboratory pack sizes, including 10 g.
- Store solid at room temperature; in solution store at -80°C or -20°C per supplier guidance.
- Comes with datasheet, certificate of analysis, and safety data sheet.
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Selleck Chemical LLC Z-VAD
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Z-VAD(OH)-FMK (Caspase Inhibitor VI) is an irreversible pan-caspase inhibitor
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Medchemexpress LLC 10-hydroxy-12(z)-octadecenoic acid | 34932-12-2 | 99.8% | 298.46 g/mol | C18H34O3 | 10 MG
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10-Hydroxy-12(Z)-octadecenoic acid is a research-grade hydroxy monounsaturated fatty acid supplied as an ester product for laboratory use. It is intended for in vitro biochemical and cellular research and is provided with supporting analytical and safety documentation.
- High purity: 99.82% reported.
- Molecular weight: 298.46 g/mol.
- Chemical formula: C18H34O3.
- CAS number: 34932-12-2.
- Supplied in small milligram pack sizes suitable for analytical and preparative work.
- Certificate of analysis (COA) and safety data sheet (SDS) available.
- Suitable as a bioactive lipid reagent for biochemical and cellular assays.
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Ambeed AMBEED
5000893589 Z-INDIRUBIN 250MG
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Medchemexpress LLC Z-pro-pro-CHO | 108708-25-4 | 98.0% | C18H22N2O4 | 10MG
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Z-Pro-Pro-CHO is a research-grade prolyl oligopeptidase inhibitor supplied as a high-purity small-molecule solid. It inhibits human prolyl oligopeptidase (IC50 0.16 μM) and Schistosoma mansoni prolyl oligopeptidase (IC50 0.01 μM), and is intended for in vitro biochemical and enzymatic studies.
- High purity, suitable for research (98.0%).
- Potent inhibitor of prolyl oligopeptidase (IC50 0.16 μM human; 0.01 μM S. mansoni).
- Characterized small-molecule with formula C18H22N2O4 and molecular weight 330.38.
- Available in milligram-scale quantities for screening and assays.
- Intended for in vitro research use only.
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Cayman Chemical 7 Z 10 Z 13 ZHexadecatrienoic
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7 Z 10 Z 13 ZHexadecatrienoic
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Medchemexpress LLC Z-aevd-fmk | 1135688-47-9 | 95.0% | 610.63 | C28H39FN4O10 | 50MG
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Z-AEVD-FMK is a peptide-based caspase-10 inhibitor used in cell biology research to block caspase-10-mediated apoptotic signaling. It inhibits activation of Bid and the mitochondrial release of apoptosis-inducing factor (AIF), resulting in reduced apoptotic cell counts in treated cultures. The compound is supplied as a solid research reagent and should be stored protected from light and under inert atmosphere; solution storage recommendations vary by solvent.
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eMolecules EMOLECULES INC
NC4013875 3 3 3-TRIFLUOROPROPANAMIDE
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AARON CHEMICALS LLC
NC3920455 3-BROMOPROPYLBENZENE
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000430836 Z -INDIRUBIN 1G
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Medchemexpress LLC (E/Z)-Polydatin ((E/Z)-Piceid) | 65914-17-2 | 98.13% | 390.38 | 1 ML
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(E/Z)-Polydatin ((E/Z)-Piceid) is a mixture of the E/Z configurations of Polydatin (HY-N0120A). Polydatin can be isolated from Polygonum cuspidatum, grapes, peanuts, red wine, hop pellets, cocoa-containing products, and chocolate products. It exhibits multiple biological properties and shows favorable cytotoxic effects against various tumor cell lines.
- Exhibits anti-platelet aggregation
- Anti-low-density lipoprotein oxidation properties
- Cardioprotective activity
- Anti-inflammatory and immunomodulatory functions
- Shows cytotoxic effects against cervical cancer cells, liver cancer cells, and nasopharyngeal carcinoma cells
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Medchemexpress LLC (Z)-FeCP-oxindole | 1137967-28-2 | 99.6% | 329.17 | 10 MM * 1 ML
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(Z)-FeCP-oxindole is a selective human vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with an IC50 value of 200 nM. It can significantly inhibit VEGFR1 and PDGFRa or b at 10 μM. (Z)-FeCP-oxindole also exhibits anticancer activity, acting on B16 murine melanoma lines with an IC50 less than 1 μM.
- Selective human vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor
- Inhibits VEGFR1 and PDGFRa or b
- Exhibits anticancer activity
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